Canonical Allele Identifier: CA557569347
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1560919530
gnomAD v2: 5-1423771-GC-G
gnomAD v3: 5-1423656-GC-G
gnomAD v4: 5-1423656-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1423660del , CM000667.2:g.1423660del GRCh38
NC_000005.9:g.1423775del , CM000667.1:g.1423775del GRCh37
NC_000005.8:g.1476775del NCBI36
NG_015885.1:g.26772del

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.654-1643del MANE Select ENSP00000270349.9:n.654-1643del
ENST00000270349.11:c.654-1643del ENSP00000270349.9:n.654-1643del
NM_001044.4:c.654-1643del NP_001035.1:n.654-1643del
NM_001044.5:c.654-1643del MANE Select NP_001035.1:n.654-1643del